These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 4092387)

  • 21. The Marinesco-Sjogren syndrome. Hereditary cerebello-lental degeneration with mental retardation.
    Alter M; Kennedy W
    Minn Med; 1968 Jul; 51(7):901-6. PubMed ID: 5658670
    [No Abstract]   [Full Text] [Related]  

  • 22. [Marinesco-Sjögren syndrome].
    Constantin F; Ionescu M
    Rev Otoneuroophtalmol; 1977; 49(1):9-11. PubMed ID: 866883
    [No Abstract]   [Full Text] [Related]  

  • 23. A somatic-nervous syndrome related to Marinesco-Sjögren's disease with some manifestations of Strümpell Lorrain's disease. Clinical report on five siblings.
    Guazzi GC; Amati A; Del Vecchio M; Di Iorio G; Fusco G
    Acta Neurol (Napoli); 1979 Apr; 1(2):101-11. PubMed ID: 474220
    [No Abstract]   [Full Text] [Related]  

  • 24. [The Marinesco-Sjögren syndrome. Preliminary anatomical verification].
    Franceschetti A; Klein D; Wildi E; Todorov A
    Schweiz Arch Neurol Neurochir Psychiatr; 1966; 97(2):234-40. PubMed ID: 5983988
    [No Abstract]   [Full Text] [Related]  

  • 25. [Peripheral neurogenic amyotrophy in the Marinesco-Sjögren syndrome].
    Serratrice G; Gastaut JL; Dubois-Gambarelli D
    Rev Neurol (Paris); 1973 Jun; 128(6):432-41. PubMed ID: 4368207
    [No Abstract]   [Full Text] [Related]  

  • 26. [Sporadic appearance of the Marinesco-Sjögren syndrome].
    Kofer J; Bejsovec M
    Cesk Neurol Neurochir; 1982 Mar; 45(2):113-6. PubMed ID: 7094097
    [No Abstract]   [Full Text] [Related]  

  • 27. [Marinesco-Sjögren syndrome].
    Tomonaga M
    Nihon Rinsho; 1977; 35 Suppl 1():544-5. PubMed ID: 612887
    [No Abstract]   [Full Text] [Related]  

  • 28. Syndrome of partial aniridia, cerebellar ataxia, and mental retardation--Gillespie syndrome.
    Nevin NC; Lim JH
    Am J Med Genet; 1990 Apr; 35(4):468-9. PubMed ID: 2333873
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Gillespie syndrome: a report of two further cases.
    Nelson J; Flaherty M; Grattan-Smith P
    Am J Med Genet; 1997 Aug; 71(2):134-8. PubMed ID: 9217210
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Myopathy of Marinesco-Sjögren syndrome. Report of a case (author's transl)].
    López Hernández A; Barrios del Valle R
    Rev Invest Clin; 1974; 26(3):277-83. PubMed ID: 4445633
    [No Abstract]   [Full Text] [Related]  

  • 31. [Pigmentary retinal degeneration, mental deterioration and ataxia: Stewart's Syndrome ].
    Calatayud T; Campos-Castello J; Negrete O; Careaga J
    Arch Neurobiol (Madr); 1982; 45(3):205-12. PubMed ID: 7125810
    [No Abstract]   [Full Text] [Related]  

  • 32. [Gillespie syndrome (incomplete aniridia, cerebellar ataxia and oligophrenia)].
    François J; Lentini F
    Klin Monbl Augenheilkd; 1984 Apr; 184(4):313-5. PubMed ID: 6727263
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Lethal familial pellagra-like skin lesion associated with neurologic and developmental impairment and the development of cataracts.
    Salih MA; Bender DA; McCreanor GM
    Pediatrics; 1985 Nov; 76(5):787-93. PubMed ID: 4058988
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Marinesco-Sjogren syndrome with myopathy.
    Chaco J
    Confin Neurol; 1969; 31(6):349-51. PubMed ID: 5386591
    [No Abstract]   [Full Text] [Related]  

  • 35. [OLIGOPHRENIA, CONGENITAL CATARACT, RETINITIS PIGMENTOSA, CEREBELLAR ATAXIA, NEUROGENIC AMYOTROPHIA. OBSERVATIONS ON 3 FAMILIAL CASES AND COMPARISON WITH THE MARINESCO-SJOGREN'S SYNDROME].
    CALVI LA
    Sist Nerv; 1963; 15():189-98. PubMed ID: 14073896
    [No Abstract]   [Full Text] [Related]  

  • 36. [Marinesco-Sjogren syndrome (personal observation and chromosome study of a case)].
    Gullo A; Cataldo F; Ficarra GG
    Pediatria (Napoli); 1972 Sep; 80(3):247-57. PubMed ID: 4680915
    [No Abstract]   [Full Text] [Related]  

  • 37. [Heredoataxia and tapetoretinal degeneration (genetic relation)].
    Boyazis RM; Hariga J; Myle G
    Encephale; 1968; 57(6):495-514. PubMed ID: 5730656
    [No Abstract]   [Full Text] [Related]  

  • 38. Dominantly inherited ataxia with abnormal urinary glycolipid content.
    Berenberg RA; Melen O; Howard GF; Harter DH
    Adv Neurol; 1984; 41():195-203. PubMed ID: 6496226
    [No Abstract]   [Full Text] [Related]  

  • 39. [Marie's ataxia with nuclear external ophthalmoplegia and muscle atrophy of lower extremities--report of an autopsy case and its family (author's transl)].
    Kurachi M; Shibata T; Koyama Y; Isaki K; Yamaguchi N
    Seishin Shinkeigaku Zasshi; 1977; 79(1):1-25. PubMed ID: 577311
    [No Abstract]   [Full Text] [Related]  

  • 40. [Marinesco-Sjogren syndrome. 1st anatomo-clinical study].
    Todorov A
    J Genet Hum; 1965 Sep; 14(2):197-233. PubMed ID: 5849252
    [No Abstract]   [Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.